Database Analyst Job in Murray Hill, NJ 07974

Title :

Database Analyst

Company :

C. R. Bard

Location :

Murray Hill, NJ 07974

Date Acquired :

7/15/2010 11:44:55 AM

Database Analyst

/Category:, Job ID:, Standard Title:, Career Level:, Location/Division:, Relocation:, Posted Date:, Close Date:">

Industry Title
/Category: Medical Device/ Clinical
Job ID: 2010-4422

Standard Title: Database Analyst
Career Level: experienced

Location/Division: Murray Hill, NJ/ Corporate
Relocation: No

Posted Date: 7/12/2010
Close Date: ..



C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare.

We expect the highest levels of quality, integrity, service, and innovation from our employees on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded.

Be Your Best at Bard and ultimately, you can have an impact on the lives of people around the world.

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More information about this job:

Overview:
The Database Analyst will be responsible for database activities for all phases of clinical development. The database analyst will lead the development and maintenance of database builds to support clinical projects / programs. He / she develops standard operating procedures and troubleshoots as required for staff regarding specific database issues. The database analyst assists with the continual process development within the data management group.


Summary of Position with General Responsibilities:
Review database design specifications;
Review CRF content vs. global object library to ensure consistency and standardization within the database;
Assists in the development of CRF and validation specifications;
Assists in performing validation procedure testing;
Design and create clinical databases, including Remote Data Capture;
Program data checks within the database and or SAS;
Develop systems for data entry and data review that comply with all relevant regulations;
Help define appropriate summaries and data presentations for internal and external use. Responsible for validation and quality assurance of any output produced for specific projects;
Develop systems for identifying error in clinical databases caused by improper data entry, protocol noncompliance and transcription error (i.e., edit checks and exception reports);
Provides technical assistance and training to programming and non-programming personnel;
Develops solutions to basic problems and assists in the development of new technologies;
Maintains all required study documentation; attends study management meetings as necessary.


Basic Qualifications:
EDUCATION:
BA / BS computer science or information technology
Proficient computer skills across multiple applications.

EXPERIENCE:
2-4 years programming experience in the device / pharmaceutical / CRO industry
Experience with development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission is required
Oracle Clinical database experience mandatory